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Reverse Transcriptase

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Reverse Transcriptase

Chemical Structure Cat. No. Product Name CAS No.
Dexelvucitabine Chemical Structure
BCP44423 Dexelvucitabine 134379-77-4
Dexelvucitabine is a nucleoside reverse transcriptase inhibitor potentially for the treatment of HIV infection.
Abacavir sulfate Chemical Structure
BCP44417 Abacavir sulfate 136777-48-5
Abacavir sulfate is an azaheterocycle sulfate salt that is the sulfate salt of the HIV-1 reverse transcriptase inhibitor abacavir. It derives from an abacavir.
Emivirine Chemical Structure
BCP43681 Emivirine 149950-60-7
Emivirine is a non-nucleoside reverse transcriptase inhibitor. Emivirine has a structure typical of a nucleoside analog but has been shown to bind directly to the reverse transcriptase and act as an NNRTI. However, it is no longer in development due to the fact that it causes an increasingly rapid breakdown of other drugs metabolized by the cytochrome P450 enzyme.
R-10015 Chemical Structure
BCP37585 R-10015 2097938-51-5
R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent and selective inhibitor of LIM domain kinase (LIMK) and binds to the ATP-binding pocket, with an IC50 of 38 nM for human LIMK1.
Nevirapine Chemical Structure
BCP05587 Nevirapine 129618-40-2
Nevirapine is a non-nucleoside inhibitor of HIV-1 reverse transcriptase used to treat and prevent HIV/AIDS; with a Ki of 270 μM.
Ro 0335 Chemical Structure
BCP28161 Ro 0335 867365-76-2
Ro-0335 is a novel diphenylether nonnucleoside reverse transcriptase inhibitor.
AVX754 Chemical Structure
BCP07907 AVX754 160707-69-7
Apricitabine, also known as (-)-BCH-10652; (-)-dOTC; AVX-754; BCH-10618; SPD-754, is an experimental nucleoside reverse transcriptase inhibitor (NRTI) against HIV.
Foscarnet sodium Chemical Structure
BCP14044 Foscarnet sodium 63585-09-1
Foscarnet Sodium inhibits viral RNA polymerases, reverse transcriptase, and DNA polymerases through noncompetitive inhibition with dNTPs.
Zidovudine Chemical Structure
BCP03622 Zidovudine 30516-87-1
Zidovudine (Retrovir) is a reverse transcriptase inhibitor.
Fangchinoline Chemical Structure
BCP26186 Fangchinoline 436-77-1
Fangchinoline is an isolate from Stephania Tetrandra that shows anti-cancer activity. It inhibits breast adenocarcinoma proliferation through apoptosis induction. In addition, it has been shown to inhibit HIV-Type 1 replication.
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